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In Vitro Dissolution Testing for Solid Oral Dosage Forms
the USP recommended ionic strength.5 For APIs that exhibit low solubilities in aqueous me-dia throughout the pH range, the addition of surfactants is recom-mended.
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FDA Guidance for Industry Dissolution Testing of Immediate, Immediate Release, Dissolution Method Development for Immediate Release, Dissolution, Dissolution Method Development for Immediate Release Solid, European Medicines Agency, RELEASE, RELEASE TESTING OF RECTAL SUPPOSITORIES CONTAINING NIMESULIDE, MULTISOURCE (GENERIC) PHARMACEUTICAL